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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284989Generated: November 1, 2026

Triphenylphosphine → 3-tert-butyl-1-(3-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)phenyl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/2284989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-(Oxan-2-yloxy)ethan-1-olHCID 4166833—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenolHCID 59557966—
SolventTetrahydrofuranHCID 8028—
Product3-tert-butyl-1-(3-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)phenyl)-1H-pyrazol-5-amineHCID 57925659—

Reaction Steps

DIAD (847 μl, 4.32 mmol) was added slowly to a solution of 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenol (US 2006/35922, which is incorporated herein by reference in its entirety; 500 mg, 2.16 mmol), 2-(tetrahydro-pyran-2-yloxy)-ethanol (439 4, 3.25 mmol) and Ph3P (1.13 g, 4.32 mmol) in THF (10.0 mL) and the mixture stirred for 72 h. The reaction mixture was partitioned between EtOAc (75 mL) and H2O (75 mL) and the aqueous layer extracted with EtOAc (3×). The combined organic layers were dried (MgSO4), filtered and evaporated in vacuo. Purification by FCC, using 5-60% EtOAc in cyclohexane, gave the title compound (1.26 g). LCMS (Method 4): Rt 2.77, m/z 360 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145413B2
Source datasetuspto-grants-2015_09
ORD IDord-e2e83e63ce534209a314f120f8100807
Source noteuspto-grants-2015_09